chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
134500891145008912AG28GENICheterozygous49745177
134500891345008914TG30GENICheterozygous49943966
134500979445009795GGT19GENICheterozygous49745182
134500979545009796CT20GENICpossibly homozygous49745183
134500984345009844GA26GENICheterozygous49943971
134501109345011094AG31GENIChomozygous49745187
134501461345014614AAT23GENICheterozygous49745211
134501461445014616TT--23GENICheterozygous49745212
134501461545014616T-23GENICheterozygous50357010
134501480745014808CCT13GENICheterozygous49943978
134501480745014808CCTT13GENICheterozygous49943979
134501609745016098AG27GENIChomozygous49745215
134501615545016156T-25GENICpossibly homozygous49745216
134501719145017192AAAC8GENICheterozygous50561440
134501719145017192AAACAC8GENICheterozygous50601817
134501918445019188ACAC----7GENICheterozygous50580096
134502128245021283TG28GENICpossibly homozygous49745245
134502382045023821A-15GENIChomozygous49745271
134502588045025881TA19GENICheterozygous49943990
134502612145026122GGTTATA20GENIChomozygous49745300
134503051745030518GA24GENIChomozygous51200674
134500979545009796CA20GENICheterozygous50494626
134501918345019184AAACACAC7GENICheterozygous50515962
134501729645017300TGTG----3GENIChomozygous50688095
134501785045017851CA14GENIChomozygous51200670
134502517745025178CCAG10GENICpossibly homozygous51200672
134502250145022505CTAT----5GENIChomozygous51233947
134503121645031217GGT30GENIChomozygous49943996
134503207645032077A-10GENIChomozygous49745400
134503220745032208A-10GENIChomozygous50688097
134503284745032848AC25GENICpossibly homozygous51200676
134503503245035033AG26GENICpossibly homozygous51200678
134503757845037579CCT21GENICheterozygous49745449
134503986545039866TTC4GENICheterozygous49745475
134503986545039866TTA4GENICheterozygous49944009
134503986845039869TTA4GENIChomozygous50688107
134503987145039872TTA4GENIChomozygous50761196
134503987445039875TTA4GENIChomozygous50550755
134503987745039878TTA3GENIChomozygous50652139